A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970108



Internal ID18258646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33079484..33081802hg38UCSC Ensembl
Innerchr6:33047261..33049579hg19UCSC Ensembl
Innerchr6:33155239..33157557hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382319
hg192319
hg182319
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2404865, nssv2404859, nssv2404862, nssv2404866, nssv2404864, nssv2404858, nssv2404861, nssv2404863, nssv2404867, nssv2404860
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesHLA-DPA1, HLA-DPB1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970108
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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